Special Drug Use Investigation for ADOAIR (Fluticasone/Sa... | NCT01395862

Studies
Special Drug Use Investigation for ADOAIR (Fluticasone/Salmeterol)

NCT01395862

Sponsor

GlaxoSmithKline

Status

Completed

Last Update Posted

Aug 21, 2013Estimated

Enrollment

1,001Actual

Phase

Not provided

Conditions

Respiratory Disorders

Interventions

Salmeterol and Fluticasone

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Aug 2013

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Nov 2007

Primary Completion Date

Sep 2012Actual

Completion Date

Sep 2012Actual

First Submitted Date

Jul 14, 2011

First Submission Date that Met QC Criteria

Jul 14, 2011

First Posted Date

Jul 18, 2011Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Aug 20, 2013

Last Update Posted Date

Aug 21, 2013Estimated

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Not provided

Is FDA Regulated Device

Not provided

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

The purpose of this study is to detect adverse drug reactions for long-term use (particularly clinically significant adverse drug reactions) occurring in clinical settings, to examine factors likely to affect the safety and efficacy in the Japanese asthma patients who are treated with fluticasone propionate/salmeterol xinafoate.

Detailed Description

Not provided

Design Module

Study Type

Observational

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not provided

Interventional Study Design

Allocation

Not provided

Intervention Model

Biospecimen

No data available

No data is available for this block.

Enrollment

1,001Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Patients prescribed fluticasone and salmeterol		Patients with asthma prescribed fluticasone and salmeterol for long-term use during study period	Drug: Salmeterol and Fluticasone

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Salmeterol and Fluticasone	Drug		Patients prescribed fluticasone and salmeterol

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
The number of incidence of adverse events in Japanese asthma patients treated with fluticasone and salmeterol for long-term		1 year

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Must use fluticasone and salmeterol for the first time
Must use fluticasone and salmeterol for long-term

Exclusion Criteria:

Patients with hypersensitivity to salmeterol and fluticasone
Patients with infection which salmeterol and fluticasone is not effective
Patients with deep mycosis

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

Not provided

Maximum Age

Not provided

Standard Ages

ChildAdultOlder Adult

Study Population

Japanese patients with asthma who are expected to use fluticasone and salmeterol for long-term.

Sampling Method

Probability Sample

Name	Affiliation	Role
GSK Clinical Trials	GlaxoSmithKline	Study Director

Condition Browse Module

MeSH Terms

ID	Term
D012120	Respiration Disorders

Ancestor Terms

ID	Term
D012140	Respiratory Tract Diseases

Browse Leaves

Not provided

Browse Branches

Not provided

Intervention Browse Module

MeSH Terms

ID	Term
D000068297	Fluticasone-Salmeterol Drug Combination

Ancestor Terms

ID	Term
D000068299	Salmeterol Xinafoate
D000420	Albuterol
D004983	Ethanolamines
D000605	Amino Alcohols

Browse Leaves

Not provided

Browse Branches

Not provided